Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion> ?p ?o ?g. }
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- NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion type Assertion NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_head.
- NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion description "[Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_provenance.
- NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion evidence source_evidence_curated NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_provenance.
- NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion SIO_000772 7981750 NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_provenance.
- NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion wasDerivedFrom uniprot-20130724 NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_provenance.
- NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_assertion wasGeneratedBy ECO_0000218 NP1180.RAT5cQWUNpWPzxs6kDpNNGJTJ7KL3IjNqOQ_fHKoXrWHs130_provenance.